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Cobalt-Catalyzed Carbozincation of Ynamides.
Sallio, Romain; Corpet, Martin; Habert, Loic; Durandetti, Muriel; Gosmini, Corinne; Gillaizeau, Isabelle.
Afiliação
  • Sallio R; Institute of Organic and Analytical Chemistry, ICOA UMR 7311 CNRS, Université d'Orléans , rue de Chartres, 45100 Orléans, France.
  • Corpet M; LCM, CNRS, Ecole polytechnique, Université Paris Saclay , 91128 Palaiseau Cedex, France.
  • Habert L; Institute of Organic and Analytical Chemistry, ICOA UMR 7311 CNRS, Université d'Orléans , rue de Chartres, 45100 Orléans, France.
  • Durandetti M; Normandie Univ, UNIROUEN, INSA Rouen, CNRS , COBRA (UMR 6014), 76000 Rouen, France.
  • Gosmini C; LCM, CNRS, Ecole polytechnique, Université Paris Saclay , 91128 Palaiseau Cedex, France.
  • Gillaizeau I; Institute of Organic and Analytical Chemistry, ICOA UMR 7311 CNRS, Université d'Orléans , rue de Chartres, 45100 Orléans, France.
J Org Chem ; 82(2): 1254-1259, 2017 01 20.
Article em En | MEDLINE | ID: mdl-28026941
An original cobalt-catalyzed ynamide carbozincation leading mainly to diverse 3-aryl enamides with mild reaction conditions and good functional-group tolerance has been developed. This reaction displays an excellent regio- and total stereoselectivity and opens the way to appealing synthetic applications. Moreover, this approach allows the selective synthesis of biologically relevant 3,5-disubstituted oxazolone frameworks.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article